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Date	Panel	Item	Activity
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08 Dec 2020	Intellectual disability - microarray and sequencing v3.643	SMARCA2	Arina Puzriakova Phenotypes for gene: SMARCA2 were changed from Nicolaides-Baraitser syndrome, 601358; COFFIN SIRIS to Nicolaides-Baraitser syndrome, OMIM:601358; Coffin-siris syndrome; Blepharophimosis intellectual disability syndrome
08 Dec 2020	Intellectual disability - microarray and sequencing v3.642	SMARCA2	Arina Puzriakova Publications for gene: SMARCA2 were set to
26 Jul 2020	Intellectual disability - microarray and sequencing v3.201	SMARCA2	Konstantinos Varvagiannis reviewed gene: SMARCA2: Rating: GREEN; Mode of pathogenicity: None; Publications: 32694869; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
29 Sep 2018	Intellectual disability - microarray and sequencing v2.468	SMARCA2	Louise Daugherty Source Victorian Clinical Genetics Services was added to SMARCA2.
02 Aug 2017	Intellectual disability - microarray and sequencing	SMARCA2	BRIDGE consortium edited their review of SMARCA2
27 Jul 2017	Intellectual disability - microarray and sequencing	SMARCA2	BRIDGE consortium edited their review of SMARCA2
19 Jul 2017	Intellectual disability - microarray and sequencing	SMARCA2	BRIDGE consortium reviewed SMARCA2